2-Iodo-N-methylacetamide

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Reagent Code: #215745
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CAS Number 83487-42-7

science Other reagents with same CAS 83487-42-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 198.99 g/mol
Formula C₃H₆INO
badge Registry Numbers
MDL Number MFCD20414908
thermostat Physical Properties
Boiling Point 299.4±23.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.935±0.06 g/cm3(Predicted)
Storage Room temperature, light-proof, inert gas

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and bioactive molecules. Its reactivity allows for the introduction of iodine functionality, which is valuable in cross-coupling reactions such as Suzuki or Heck reactions. Commonly employed in the development of radiolabeled compounds for medicinal imaging and tracer studies due to the presence of iodine, which can be easily substituted with radioactive isotopes. Also serves as a building block in the synthesis of peptides and modified amino acids, where the iodo group enables further functionalization. Its methylamide structure enhances stability and solubility in various solvents, making it suitable for multistep synthetic routes in drug discovery.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,850.00
inventory 250mg
10-20 days ฿11,640.00
inventory 1g
10-20 days ฿31,380.00

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2-Iodo-N-methylacetamide
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and bioactive molecules. Its reactivity allows for the introduction of iodine functionality, which is valuable in cross-coupling reactions such as Suzuki or Heck reactions. Commonly employed in the development of radiolabeled compounds for medicinal imaging and tracer studies due to the presence of iodine, which can be easily substituted with radioactive isotopes. Also serves as a building block in the synthe

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and bioactive molecules. Its reactivity allows for the introduction of iodine functionality, which is valuable in cross-coupling reactions such as Suzuki or Heck reactions. Commonly employed in the development of radiolabeled compounds for medicinal imaging and tracer studies due to the presence of iodine, which can be easily substituted with radioactive isotopes. Also serves as a building block in the synthesis of peptides and modified amino acids, where the iodo group enables further functionalization. Its methylamide structure enhances stability and solubility in various solvents, making it suitable for multistep synthetic routes in drug discovery.

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